OMOP Concept 135061
Congenital anomaly of musculoskeletal system
StandardConditionSNOMED73573004Disorder
Maps from
65
Descendants
2,453
Valid from
31 Jan 2002
Valid to
31 Dec 2099
OMOP concepts
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Source codes that map to this concept
65 source codes normalize to Congenital anomaly of musculoskeletal system via the OMOP "Maps to" relationship.
Synonyms
Alternative names recorded for Congenital anomaly of musculoskeletal system across source vocabularies.
- anomalía congénita del sistema musculoesquelético
- anomalía congénita del sistema musculoesquelético (trastorno)
- anomalía musculoesquelética congénita
- Congenital abnormality of musculoskeletal system
- Congenital anomaly of musculoskeletal system (disorder)
- Congenital malformation of musculoskeletal system
- Congenital musculoskeletal abnormality
- malformación congénita del sistema musculoesquelético
Where it sits in the hierarchy
Ordered by distance - 1 is a direct parent or child.
Broader concepts
(9)Roll up to these when you need a wider cohort.
Narrower concepts
(2,453)Included automatically when you query with descendants.
- 18q24.3 microdeletion syndrome
- 1Absent thumb with short stature and immunodeficiency syndrome
- 1Acrania
- 1Aplasia of bone of axial skeleton
- 1Aplasia of muscle
- 1BSG syndrome
- 1Cleft palate with short stature and vertebral anomaly syndrome
- 1CLOVE syndrome
- 1Coffin-Lowry syndrome
- 1Congenital absence of cranial vault
- 1Congenital anomaly of cartilage
- 1Congenital anomaly of joint
- 1Congenital anomaly of muscle AND/OR tendon
- 1Congenital anomaly of musculoskeletal structure of trunk
- 1Congenital anomaly of skeletal bone
- 1Congenital claw foot
- 1Congenital deformity of musculoskeletal system
- 1Congenital hyperplasia of muscle
- 1Congenital instability of spine
- 1Congenital radial deviation of finger
- 1Congenital sacrococcygeal anomaly
- 1Failure of soft tissue differentiation of lower limb
- 1Hypoplasia of spine
- 1Macrocephaly, intellectual disability, left ventricular non compaction syndrome
- 1Marfanoid habitus, facial dysmorphism, skeletal abnormality, heart defect syndrome
- 1Myostatin related hypertrophy of muscle
- 1Neurodevelopmental disorder, craniofacial dysmorphism, cardiac defect, skeletal anomalies syndrome
- 1Night blindness, skeletal anomalies, dysmorphism syndrome
- 1Overgrowth syndrome with 2q37 translocation
- 1Skeletal dysplasia
- 1Syndactyly of toes with fusion of bones
- 1Talipomanus
- 1Trichorhinophalangeal dysplasia type I
- 1Trichorhinophalangeal dysplasia type III
- 1Trichorhinophalangeal syndrome type 1 and 3
- 1Windblown hand
- 23-M syndrome
- 246,XX disorder of sex development with skeletal anomalies syndrome
- 2Accessory ossification center
- 2Achondrogenesis
- 2Achondrogenesis, type IA
- 2Achondrogenesis, type IB
- 2Acrodysplasia scoliosis
- 2Acromesomelic dysplasia syndrome
- 2Agenesis of hyoid bone
- 2Agenesis of nasal cartilages
- 2Agenesis of premaxilla
- 2Alkuraya Kucinskas syndrome
- 2Angel-shaped phalangoepiphyseal dysplasia
- 2Angio-osteohypertrophic syndrome
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